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MECLIZINE HYDROCHLORIDE

MECLIZINE HYDROCHLORIDE · 25MG · TABLET · ORAL

ANDA084092HUMAN PRESCRIPTION DRUG
Open FDA's page for this record
Approval date
19890522
Product number
003
Products
  1. Brand name
    MECLIZINE HYDROCHLORIDE
    Application name
    QUAGEN
    Application type
    A
    Application number
    084092
    Reference listed drug
    false
    Reference standard
    false
    Marketing status
    HUMAN PRESCRIPTION DRUG
    Application full name
    QUAGEN PHARMACEUTICALS LLC
    Dosage form
    TABLET
    Route
    ORAL
    Active ingredients
    1. Name
      MECLIZINE HYDROCHLORIDE
      Strength
      25MG
    Therapeutic equivalence codes
    AA
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.